Variant #0000316622 (NC_000002.11:g.219132388T>C, NC_000002.11(NM_001087.3):c.275-52A>G (AAMP))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.219132388T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAMP_000084
Frequency 11/7272
Freq. EA 0/4618
Freq. AA 11/2654
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:22:05 +02:00 (CEST)
Date last edited 2018-08-23 01:53:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAMP NM_001087.3 ?/? c.275-52A>G r.(=) p.(=)